Facile conversion of natural colchicine into (±)-congeners and (+)-enantiomers including 2-demethyl analogues

DOI: 10.1021/jo00363a021

Source and publish data:

Journal of Organic Chemistry p. 2515 - 2521 (1986)

Update date:2022-08-05

Topics: Facile conversion

Authors:

Dumont Dumont

Brossi Brossi

Silverton

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/jo00363a021

Full text of DOI:10.1021/jo00363a021

Products guided by the article

Product name:(R)-N-Deacetyl Colchicine

Cas No:102419-91-0

R&D Labs maybe for 102419-91-0

PharmOrgsyn

Contact:+86-21-38228826

Address:Room 505 Building 2, No 3377 Kangxin Highway, Shanghai, Republic China
Chengdu Green Young Biopharmaceutical INC

Contact:+86-28-85337952

Address:1-B-26,Tianhe Industry Park, No.1480 of Tianfu Road,Chengdu,P.R.China,610000
YanCheng LongShen Chemical Co.,Ltd.

Contact:+86-515-86668866

Address:No.13,Weiyi Road,Funing Aoyang Industrial Park
Wuhan Yitongtai Science and Technology Co.,Ltd.

Contact:+86-27-88933550

Address:27th Fl. Bldg. 1, Shuian International Mansion, Heping Ave, Wuhan, Hubei, China
Chameleon Specialty Chemicals

Contact:+44 7958 511245

Address:PO Box 469, Manchester, UK

Relevant to this article

HIGHLY ENANTIOSELECTIVE REDUCTION OF δ-KETO ACIDS WITH FERMENTING BAKER'S YEAST. A FACILE SYNTHESIS OF OPTICALLY PURE (R)-(+)-5-HEXADECANOLIDE

Doi:10.1246/cl.1985.1475
(1985)
β-CARBONYL RADICALS AS THREE-CARBON BUILDING BLOCKS FOR CARBON-CARBON BOND FORMING REACTIONS

Doi:10.1016/S0040-4020(01)97181-9
(1985)
Phenylethynyl-pyrrolo[1,2-a]pyrazine: A new potent and selective tool in the mGluR5 antagonists arena

Doi:10.1016/j.bmcl.2008.02.024
(2008)
LDA-mediated selective addition reaction of vinylidenecyclopropanes with aldehydes, ketones, and enones: Facile synthesis of vinylcyclopropenes allenols, and 1,3-enynes

Doi:10.1021/ol800463k
(2008)
Potent, nonpeptide inhibitors of human mast cell tryptase. Synthesis and biological evaluation of novel spirocyclic piperidine amide derivatives

Doi:10.1016/j.bmcl.2008.01.093
(2008)
Bioactive products from singlet oxygen photooxygenation of cannabinoids

Doi:10.1016/j.ejmech.2017.11.043
(2018)

Article Doi